Biology:Brain natriuretic peptide 32

From HandWiki
Short description: Hormone secreted in the heart

Brain natriuretic peptide 32 (BNP), also known as B-type natriuretic peptide, is a hormone secreted by cardiomyocytes in the heart ventricles in response to stretching caused by increased ventricular blood volume.[1] BNP is one of the three natriuretic peptides, in addition to ANP and CNP. [2]

The 32-amino acid polypeptide BNP is secreted attached to a 76–amino acid N-terminal fragment in the prohormone called NT-proBNP (BNPT), which is biologically inactive. Once released, BNP binds to and activates the atrial natriuretic factor receptor NPRA, and to a lesser extent NPRB, in a fashion similar to atrial natriuretic peptide (ANP) but with 10-fold lower affinity. The biological half-life of BNP, however, is twice as long as that of ANP, and that of NT-proBNP is even longer, making these peptides better targets than ANP for diagnostic blood testing.

The physiologic actions of BNP are similar to those of ANP and include decrease in systemic vascular resistance and central venous pressure as well as an increase in natriuresis. The net effect of these peptides is a decrease in blood pressure due to the decrease in systemic vascular resistance and, thus, afterload. Additionally, the actions of both BNP and ANP result in a decrease in cardiac output due to an overall decrease in central venous pressure and preload as a result of the reduction in blood volume that follows natriuresis and diuresis.[3]

Biosynthesis

BNP is synthesized as a 134-amino acid preprohormone (preproBNP), encoded by the human gene NPPB. Removal of the 25-residue N-terminal signal peptide generates the prohormone, proBNP, which is stored intracellularly as an O-linked glycoprotein; proBNP is subsequently cleaved between arginine-102 and serine-103 by a specific convertase (probably furin or corin) into NT-proBNP and the biologically active 32-amino acid polypeptide BNP-32, which are secreted into the blood in equimolar amounts.[4] Cleavage at other sites produces shorter BNP peptides with unknown biological activity.[5] Processing of proBNP may be regulated by O-glycosylation of residues near the cleavage sites.[6] The synthesis of BNP in cardiomyocytes is stimulated by pro-inflammatory cell factors, such as interleukin-1β, interleukin-6 and tumor necrosis factor-α.[7]

Physiologic effects

Renal

  • Dilates the afferent glomerular arteriole, constricts the efferent glomerular arteriole, and relaxes the mesangial cells. This increases pressure in the glomerular capillaries, thus increasing the glomerular filtration rate (GFR), resulting in greater filter load of sodium and water.
  • Increases blood flow through the vasa recta, which will wash the solutes (NaCl and urea) out of the medullary interstitium.[8] The lower osmolarity of the medullary interstitium leads to less reabsorption of tubular fluid and increased excretion.
  • Decreases sodium reabsorption in the distal convoluted tubule (interaction with NCC)[9] and cortical collecting duct of the nephron via guanosine 3',5'-cyclic monophosphate (cGMP) dependent phosphorylation of ENaC.
  • Inhibits renin secretion, thereby inhibiting the renin–angiotensin–aldosterone system.

Adrenal

  • Reduces aldosterone secretion by the zona glomerulosa of the adrenal cortex.

Vascular

Relaxes vascular smooth muscle in arterioles and venules by:

  • Membrane Receptor-mediated elevation of vascular smooth muscle cGMP
  • Inhibition of the effects of catecholamines

Promotes uterine spiral artery remodeling, which is important for preventing pregnancy-induced hypertension.[10]

Cardiac

  • Inhibits maladaptive cardiac hypertrophy
  • Mice lacking cardiac NPRA develop increased cardiac mass and severe fibrosis and die suddenly[11]
  • Re-expression of NPRA rescues the phenotype.

Adipose tissue

  • Increases the release of free fatty acids from adipose tissue. Plasma concentrations of glycerol and nonesterified fatty acids are increased by i.v. infusion of ANP in humans.
  • Activates adipocyte plasma membrane type A guanylyl cyclase receptors NPR-A
  • Increases intracellular cGMP levels that induce the phosphorylation of a hormone-sensitive lipase and perilipin A via the activation of a cGMP-dependent protein kinase-I (cGK-I)
  • Does not modulate cAMP production or PKA activity

Measurement

BNP and NT-proBNP are measured by immunoassay.[12]

Interpretation of BNP

  • The main clinical utility of either BNP or NT-proBNP is that a normal level helps to rule out chronic heart failure in the emergency setting. An elevated BNP or NT-proBNP should never be used exclusively to "rule in" acute or chronic heart failure in the emergency setting due to lack of specificity [dubious – discuss].[13]
  • Either BNP or NT-proBNP can also be used for screening and prognosis of heart failure.[14]
  • Increased NT-proBNP adjusted for age and sex and annual increase of NT-proBNP above 50% are associated with increased event rate in patients with non-severe aortic valve stenosis.[15]
  • BNP and NT-proBNP are also typically increased in patients with left ventricular dysfunction, with or without symptoms (BNP accurately reflects current ventricular status, as its half-life is 20 minutes, as opposed to 1–2 hours for NT-proBNP).[16]

A preoperative BNP can be predictive of a risk of an acute cardiac event during vascular surgery. A cutoff of 100 pg/ml has a sensitivity of approximately 100%, a negative predictive value of approximately 100%, a specificity of 90%, and a positive predictive value of 78% according to data from the United Kingdom .[17]

BNP is cleared by binding to natriuretic peptide receptors (NPRs) and neutral endopeptidase (NEP). Less than 5% of BNP is cleared renally. NT-proBNP is the inactive molecule resulting from cleavage of the prohormone Pro-BNP and is reliant solely on the kidney for excretion. The achilles heel of the NT-proBNP molecule is the overlap in kidney disease in the heart failure patient population.[18][19]

Some laboratories report in units ng per Litre (ng/L), which is equivalent to pg/mL

There is a diagnostic 'gray area', often defined as between 100 and 500 pg/mL, for which the test is considered inconclusive, but, in general, levels above 500 pg/ml are considered to be an indicator of heart failure. This so-called gray zone has been addressed in several studies, and using clinical history or other available simple tools can help make the diagnosis.[20][21]

BNP has been suggested as a predictor for a variety of medical states, including cardiovascular mortality in diabetics[22] and cardiac impairment in cancer patients.[23][24]

BNP was found to have an important role in prognostication of heart surgery patients[25] and in the emergency department.[26] Bhalla et al. showed that combining BNP with other tools like ICG can improve early diagnosis of heart failure and advance prevention strategies.[27][28] Utility of BNP has also been explored in various settings like preeclampsia, ICU and shock and ESRD.[29][30][31]

The effect or race and gender on value of BNP and its utility in that context has been studied extensively.[32][33]

NT-proBNP levels (in pg/mL) by NYHA functional class[34]
NYHA I NYHA II NYHA III NYHA IV
5th Percentile 33 103 126 148
Mean 1015 1666 3029 3465
95th Percentile 3410 6567 10,449 12,188

The BNP test is used as an aid in the diagnosis and assessment of severity of heart failure. A recent meta-analysis concerning effects of BNP testing on clinical outcomes of patients presenting to the emergency department with acute dyspnea revealed that BNP testing led to a decrease in admission rates and decrease in mean length of stay, although neither was statistically significant. Effects on all cause hospital mortality was inconclusive.[35] The BNP test is also used for the risk stratification of patients with acute coronary syndromes.[36][37]

When interpreting an elevated BNP level, values may be elevated due to factors other than heart failure. Lower levels are often seen in obese patients.[38] Higher levels are seen in those with renal disease, in the absence of heart failure.

Therapeutic application

Recombinant BNP, nesiritide, has been suggested as a treatment for decompensated heart failure. However, a clinical trial failed to show a benefit of nesiritide in patients with acute decompensated heart failure.[39] Blockade of neprilysin, a protease known to degrade members of the natriuretic peptide family, has also been suggested as a possible treatment for heart failure. Dual administration of neprilysin inhibitors and angiotensin receptor blockers has been shown to be advantageous to ACE inhibitors, the current first-line therapy, in multiple settings.[40][41]

See also

References

  1. ↑ Potter, LR; Yoder, AR; Flora, DR; Antos, LK; Dickey, DM (2009). Natriuretic peptides: their structures, receptors, physiologic functions and therapeutic applications.. Handbook of Experimental Pharmacology. 191. pp. 341–66. doi:10.1007/978-3-540-68964-5_15. ISBN 978-3-540-68960-7. 
  2. ↑ Potter, Lincoln R.; Yoder, Andrea R.; Flora, Darcy R.; Antos, Laura K.; Dickey, Deborah M. (2009). "Natriuretic Peptides: Their Structures, Receptors, Physiologic Functions and Therapeutic Applications". Handbook of Experimental Pharmacology 191 (191): 341–366. doi:10.1007/978-3-540-68964-5_15. ISBN 978-3-540-68960-7. ISSN 0171-2004. PMID 19089336. 
  3. ↑ "CV Pharmacology - Natriuretic Peptides". http://cvpharmacology.com/diuretic/natriuretics. 
  4. ↑ "The precursor to B-type natriuretic peptide is an O-linked glycoprotein". Archives of Biochemistry and Biophysics 451 (2): 160–6. July 2006. doi:10.1016/j.abb.2006.03.028. PMID 16750161. 
  5. ↑ "Detection of endogenous B-type natriuretic peptide at very low concentrations in patients with heart failure". Circulation: Heart Failure 1 (4): 258–64. November 2008. doi:10.1161/CIRCHEARTFAILURE.108.790774. PMID 19808300. 
  6. ↑ "Processing of pro-brain natriuretic peptide is suppressed by O-glycosylation in the region close to the cleavage site". Clinical Chemistry 55 (3): 489–98. March 2009. doi:10.1373/clinchem.2008.113373. PMID 19168558. 
  7. ↑ Fu, Shihui; Ping, Ping; Wang, Fengqi; Luo, Leiming (December 2018). "Synthesis, secretion, function, metabolism and application of natriuretic peptides in heart failure". Journal of Biological Engineering 12 (1): 2. doi:10.1186/s13036-017-0093-0. PMID 29344085. 
  8. ↑ "Effect of atrial natriuretic peptide on vasa recta blood flow in the rat". The American Journal of Physiology 252 (6 Pt 2): F1112-7. June 1987. doi:10.1152/ajprenal.1987.252.6.F1112. PMID 2954471. 
  9. ↑ "Chapter 31 – Sodium Chloride Transport in the Loop of Henle, Distal Convoluted Tubule, and Collecting Duct". Seldin and Giebisch's the kidney: physiology and pathophysiology. Amsterdam: Elsevier/Academic Press. 2008. pp. 849–887. doi:10.1016/B978-012088488-9.50034-6. ISBN 978-0-12-088488-9. https://archive.org/details/seldingiebischsk00alpe. 
  10. ↑ "Role of corin in trophoblast invasion and uterine spiral artery remodelling in pregnancy". Nature 484 (7393): 246–50. March 2012. doi:10.1038/nature10897. PMID 22437503. Bibcode: 2012Natur.484..246C. 
  11. ↑ "Cardiac fibrosis in mice lacking brain natriuretic peptide". Proceedings of the National Academy of Sciences of the United States of America 97 (8): 4239–44. April 2000. doi:10.1073/pnas.070371497. PMID 10737768. Bibcode: 2000PNAS...97.4239T. 
  12. ↑ "State of the art of BNP and NT-proBNP immunoassays: the CardioOrmoCheck study". Clinica Chimica Acta; International Journal of Clinical Chemistry 414: 112–9. December 2012. doi:10.1016/j.cca.2012.07.017. PMID 22910582. 
  13. ↑ "Rapid measurement of B-type natriuretic peptide in the emergency diagnosis of heart failure". The New England Journal of Medicine 347 (3): 161–7. July 2002. doi:10.1056/NEJMoa020233. PMID 12124404. 
  14. ↑ "B-type natriuretic peptide: the level and the drug--partners in the diagnosis of congestive heart failure". Congestive Heart Failure 10 (1 Suppl 1): 3–27. 2004. doi:10.1111/j.1527-5299.2004.03310.x. PMID 14872150. 
  15. ↑ Hadziselimovic, Edina; Greve, Anders M.; Sajadieh, Ahmad; Olsen, Michael H.; Kesäniemi, Y. Antero; Nienaber, Christoph A.; Ray, Simon G.; Rossebø, Anne B. et al. (2022-04-01). "Association of Annual N-Terminal Pro-Brain Natriuretic Peptide Measurements With Clinical Events in Patients With Asymptomatic Nonsevere Aortic Stenosis: A Post Hoc Substudy of the SEAS Trial" (in en). JAMA Cardiology 7 (4): 435–444. doi:10.1001/jamacardio.2021.5916. ISSN 2380-6583. PMID 35171199. PMC 8851368. https://jamanetwork.com/journals/jamacardiology/fullarticle/2788912. 
  16. ↑ "A prospective study in search of an optimal B-natriuretic peptide level to screen patients for cardiac dysfunction". American Heart Journal 148 (3): 518–23. September 2004. doi:10.1016/j.ahj.2004.03.014. PMID 15389242. 
  17. ↑ "Predictive value of plasma brain natriuretic peptide for cardiac outcome after vascular surgery". Heart 92 (3): 401–2. March 2006. doi:10.1136/hrt.2005.060988. PMID 16501204. 
  18. ↑ "Correlation and prognostic utility of B-type natriuretic peptide and its amino-terminal fragment in patients with chronic kidney disease". American Journal of Clinical Pathology 126 (4): 506–12. October 2006. doi:10.1309/M7AAXA0J1THMNCDF. PMID 16938661. 
  19. ↑ "How obesity affects the cut-points for B-type natriuretic peptide in the diagnosis of acute heart failure. Results from the Breathing Not Properly Multinational Study". American Heart Journal 151 (5): 999–1005. May 2006. doi:10.1016/j.ahj.2005.10.011. PMID 16644321. 
  20. ↑ "Impact of the history of congestive heart failure on the utility of B-type natriuretic peptide in the emergency diagnosis of heart failure: results from the Breathing Not Properly Multinational Study". The American Journal of Medicine 119 (1): 69.e1–11. January 2006. doi:10.1016/j.amjmed.2005.04.029. PMID 16431187. 
  21. ↑ "Gray zone BNP levels in heart failure patients in the emergency department: results from the Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT) multicenter study". American Heart Journal 151 (5): 1006–11. May 2006. doi:10.1016/j.ahj.2005.10.017. PMID 16644322. 
  22. ↑ "Prognostic role of B-type natriuretic peptide levels in patients with type 2 diabetes mellitus". Journal of the American College of Cardiology 44 (5): 1047–52. September 2004. doi:10.1016/j.jacc.2004.05.071. PMID 15337217. 
  23. ↑ Palumbo, I.Expression error: Unrecognized word "etal". (2016). "Brain natriuretic peptide as a cardiac marker of transient radiotherapy-related damage in left-sided breast cancer patients: A prospective study". The Breast 25: 45–50. doi:10.1016/j.breast.2015.10.004. PMID 26547836. 
  24. ↑ Bando, S.Expression error: Unrecognized word "etal". (2017). "Plasma brain natriuretic peptide levels are elevated in patients with cancer". PLOS ONE 12 (6): e0178607. doi:10.1371/journal.pone.0178607. PMID 28570595. Bibcode: 2017PLoSO..1278607B. 
  25. ↑ "Utility of B-type natriuretic peptide in predicting postoperative complications and outcomes in patients undergoing heart surgery". Journal of the American College of Cardiology 43 (10): 1873–9. May 2004. doi:10.1016/j.jacc.2003.12.048. PMID 15145114. 
  26. ↑ "Primary results of the Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT). A multicenter study of B-type natriuretic peptide levels, emergency department decision making, and outcomes in patients presenting with shortness of breath". Journal of the American College of Cardiology 44 (6): 1328–33. September 2004. doi:10.1016/j.jacc.2004.06.015. PMID 15364340. 
  27. ↑ "Diagnostic ability of B-type natriuretic peptide and impedance cardiography: testing to identify left ventricular dysfunction in hypertensive patients". American Journal of Hypertension 18 (2 Pt 2): 73S–81S. February 2005. doi:10.1016/j.amjhyper.2004.11.044. PMID 15752936. 
  28. ↑ "B-type natriuretic peptide and impedance cardiography at the time of routine echocardiography predict subsequent heart failure events". Journal of Cardiac Failure 15 (1): 41–7. February 2009. doi:10.1016/j.cardfail.2008.09.003. PMID 19181293. 
  29. ↑ "Evaluation of B-type natriuretic peptide (BNP) levels in normal and preeclamptic women". American Journal of Obstetrics and Gynecology 193 (2): 450–4. August 2005. doi:10.1016/j.ajog.2004.12.006. PMID 16098869. 
  30. ↑ "Evolution of B-type natriuretic peptide in evaluation of intensive care unit shock". Critical Care Medicine 32 (8): 1787–9. August 2004. doi:10.1097/01.CCM.0000135748.75590.54. PMID 15286561. 
  31. ↑ "The use of B-type natriuretic peptide to assess volume status in patients with end-stage renal disease". American Heart Journal 153 (2): 244.e1–5. February 2007. doi:10.1016/j.ahj.2006.10.041. PMID 17239684. 
  32. ↑ "Impact of age, race, and sex on the ability of B-type natriuretic peptide to aid in the emergency diagnosis of heart failure: results from the Breathing Not Properly (BNP) multinational study". American Heart Journal 147 (6): 1078–84. June 2004. doi:10.1016/j.ahj.2004.01.013. PMID 15199359. 
  33. ↑ "B-type natriuretic peptide (BNP) levels and ethnic disparities in perceived severity of heart failure: results from the Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT) multicenter study of BNP levels and emergency department decision making in patients presenting with shortness of breath". Journal of Cardiac Failure 12 (4): 281–5. May 2006. doi:10.1016/j.cardfail.2006.01.008. PMID 16679261. 
  34. ↑ "N-terminal-pro-BNP". LABORATORY SERVICES HANDBOOK. The University of Iowa (UIHC), Department of Pathology. 28 May 2020. https://www.healthcare.uiowa.edu/path_handbook/handbook/test2621.html.  Showing 95th percentiles. Epic Lab Code: LAB649.
  35. ↑ "Meta-analysis: effect of B-type natriuretic peptide testing on clinical outcomes in patients with acute dyspnea in the emergency setting". Annals of Internal Medicine 153 (11): 728–35. December 2010. doi:10.7326/0003-4819-153-11-201012070-00006. PMID 21135296. 
  36. ↑ "N-terminal fragment of the prohormone brain-type natriuretic peptide (NT-proBNP), cardiovascular events, and mortality in patients with stable coronary heart disease". JAMA 297 (2): 169–76. January 2007. doi:10.1001/jama.297.2.169. PMID 17213400. 
  37. ↑ "Effect of nesiritide in combination with standard therapy on serum concentrations of natriuretic peptides in patients admitted for decompensated congestive heart failure". American Heart Journal 150 (3): 471–7. September 2005. doi:10.1016/j.ahj.2004.11.021. PMID 16169326. 
  38. ↑ "Impact of obesity on plasma natriuretic peptide levels". Circulation 109 (5): 594–600. February 2004. doi:10.1161/01.CIR.0000112582.16683.EA. PMID 14769680. 
  39. ↑ "Effect of nesiritide in patients with acute decompensated heart failure". The New England Journal of Medicine 365 (1): 32–43. July 2011. doi:10.1056/NEJMoa1100171. PMID 21732835. https://iris.unibs.it/bitstream/11379/60663/1/ASCEND-HF%20NEJM%202011.pdf. 
  40. ↑ "Angiotensin-neprilysin inhibition versus enalapril in heart failure". The New England Journal of Medicine 371 (11): 993–1004. September 2014. doi:10.1056/NEJMoa1409077. PMID 25176015. http://www.hirsla.lsh.is/lsh/handle/2336/552372. 
  41. ↑ "Angiotensin-Neprilysin Inhibition in Acute Decompensated Heart Failure". The New England Journal of Medicine 380 (6): 539–548. February 2019. doi:10.1056/NEJMoa1812851. PMID 30415601. 

Further reading

External links

attribution: copied from Brain natriuretic peptide version as of 13:57, 4 December 2019



Retrieved from "https://handwiki.org/wiki/index.php?title=Biology:Brain_natriuretic_peptide_32&oldid=3600125"